A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526697



Internal ID15453990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133128302..133167633hg38UCSC Ensembl
Innerchr8:134140546..134179877hg19UCSC Ensembl
Innerchr8:134209728..134249059hg18UCSC Ensembl
Innerchr8:134209728..134249059hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3839332
hg1939332
hg1839332
hg1739332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703035
Samples
Known GenesTG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526697
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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